**Join Amgen’s Mission of Serving Patients** At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Specialist QA **What you will do** Let’s do this. Let’s change the world. In this role you will have the opportunity to be part of the continued expansion of Quality Operations at Amgen Ohio (AOH) supporting our growing state-of-the-art Final Drug Product (FDP) Plant. You will lead and direct cross functional staff as an informed Subject Matter Expert in the Quality deliverables. A key aspect of this role is to apply critical thinking skills to ensure quality and compliance to GMP regulations for operations and associated processes. Duties include oversight on daily manufacturing operations, development and approval of standard operating procedure, quality approval of deviations and final batch disposition. Responsibilities will include evaluation of compliance and quality issues, providing recommendations for improvement projects, and assuring progress of records to completion. + Review and approve controlled documents, including Standard Operating Procedures, Validation Protocols, Validation Reports, Electronic Master Batch Records etc. + Provide quality oversight for quality records including deviations/CAPAs, technical change controls and work orders assuring adherence to procedural requirements and confirming assessments and evaluations of different partners are complete and accurate + Ensure that all activities & related documentation for facilities, equipment, materials and processes align with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and Controls. + Own quality related Standard Operating Procedures, Work Instructions, Forms and Methods + Provide quality oversight for manufacturing and be responsible for batch disposition. + Provide quality and compliance expertise & guidance and agrees on strategies related to the design, installation, commissioning & qualification and process qualification of the new facility, equipment and information systems. + Support and represent Quality during audits and inspections; may directly interact with regulatory agencies during on-site inspections. + Support Lean Transformation and Operational Excellence initiatives **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The Quality professional we seek is a dynamic, flexible and driven individual with these qualifications **Basic Qualifications:** Doctorate degree Or Master’s degree and 2 years of Quality and/or Manufacturing experience Or Bachelor’s degree and 4 years of Quality and/or Manufacturing experience Or Associate’s degree and 8 years of Quality and/or Manufacturing experience Or High school diploma / GED and 10 years of Quality and/or Manufacturing experience **Preferred Qualifications:** + Master's or Bachelor’s Degree in Science + Educated in a science field with 5 years of experience in GMP/GCP operations or similarly regulated industry + Affinity with digital innovation, data sciences and Quality engineering + Experience in review/approval validation documentation + Ability to complete tasks autonomously, providing updates to senior management, and identifying potential issues + Ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations + Experience working with dynamic cross-functional teams and abilities in decision making + Strong organizational skills, including ability to follow assignments through to completion + Strong leadership capabilities and experience applying GMP requirements in an operational setting + Ability to independently interact with various levels, drives tasks to completion, and is a self-starter. **What you can expect from us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models, including remote and hybrid work arrangements, where possible **Apply now** **for a career that defies imagination** Objects in your future are closer than they appear. Join us. **careers.amgen.com** In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.